Chapter 15: Q1. (page 570)
Question: Classify each radical as Primary , secondary or tertiary carbon radicals .
Short Answer
Answer
a. carbon radical
b. carbon radical
c. carbon radical
d. localid="1648713761224" carbon radical
Chapter 15: Q1. (page 570)
Question: Classify each radical as Primary , secondary or tertiary carbon radicals .
Answer
a. carbon radical
b. carbon radical
c. carbon radical
d. localid="1648713761224" carbon radical
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Question:Treatment of a hydrocarbon A (molecular formula C9H18) with Br2 in the presence of light forms alkyl halides B and C, both having molecular formula C9H17Br. Reaction of either B or C with KOC (CH3)3 forms compound D ( C9H16) as the major product. Ozonolysis of D forms cyclohexanone and acetone. Identify the structures of A–D.


Question: With reference to the indicated C-H bonds in 2-methylbutane.
a. Rank the C-H bonds in order of increasing bond length.
b. Draw the radical resulting from cleavage of each C-H bond and classify it as 10,20, or 30
c.Rank the order of radicals in order of increasing stability.
Rank the C-H bonds in order of increasing ease of H abstractions in a radical halogenation reaction.
Question: Devise a synthesis of each compound using CH3CH3 as the only source of carbon atoms. You may use any other required organic or inorganic reagents.
a.

b.

c.

d.

Question: Identify the structure of a minor product formed from the radical chlorination of propane, which has molecular formula C3H6Cl2 and exhibits the given 1H NMR spectrum.

Question:Draw the products formed in each reaction and include the stereochemistry around any stereogenic centers.
a.

b.

c.

d.

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